Exhibit 99.15

Johnson  & Johnson Reports 2007 Third-Quarter Results:  Sales  of
$15.0  Billion  Increased 12.7%; EPS was $.88, Including  Special
Charges; Excluding Special Charges, EPS was $1.06 *

NEW  BRUNSWICK,  N.J.,  Oct  16, 2007  /PRNewswire-FirstCall  via
COMTEX  News  Network/  -- Johnson & Johnson  (NYSE:  JNJ)  today
announced  third-quarter sales of $15.0 billion, an  increase  of
12.7%  as  compared  to  the third quarter of  2006.  Operational
growth  was  9.7% and currency contributed 3.0%.  Domestic  sales
were   up  5.8%,  while  international  sales  increased   21.5%,
reflecting  operational growth of 14.7% and a  positive  currency
impact of 6.8%. On a pro-forma basis, including the net impact of
the  acquisition of Pfizer Consumer Healthcare in  both  periods,
worldwide sales increased 2.4% operationally.

Net earnings and diluted earnings per share for the third quarter
of  2007  were  $2.5 billion and $.88, representing decreases  of
7.7% and 6.4%, respectively, compared to the same period in 2006.
Net   earnings  for  the  third  quarter  included  an  after-tax
restructuring  charge of $528 million associated  with  the  cost
improvement  program previously announced on  July  31st.  Prior-
year  third-quarter  net earnings included  after-tax  in-process
research and development charges of $115 million associated  with
the  acquisitions of Ensure Medical, Inc. and Colbar  LifeScience
Ltd. Excluding the impact of these charges, net earnings for  the
current quarter were $3.1 billion and diluted earnings per  share
were   $1.06,   representing  increases   of   7.0%   and   8.2%,
respectively,  as  compared  to the same  period  in  2006.*  The
Company increased its earnings guidance for full-year 2007, which
excludes  the  impact  of  in- process research  and  development
charges, restructuring charges or other special items, to between
$4.10 and $4.13 per share.

"We  continue  to deliver solid earnings while investing  in  the
future  growth of our business," said William C. Weldon, Chairman
and Chief Executive Officer. "Our broad base enables us to pursue
opportunities  while  managing  through  pressures   in   certain
markets."

Worldwide  Medical Devices and Diagnostics sales of $5.2  billion
for  the third quarter represented a 6.0% increase over the prior
year  with operational growth of 3.0% and a positive impact  from
currency   of   3.0%.  Domestic  sales  increased   2.4%,   while
international sales increased 9.8% (3.7% from operations and 6.1%
from currency).

Primary   contributors   to  the  operational   growth   included
Vistakon's  disposable contact lenses; LifeScan's  blood  glucose
monitoring  and  insulin delivery products;  DePuy's  orthopaedic
joint  reconstruction and sports medicine products; Ethicon Endo-
Surgery's   minimally  invasive  products;   and   Ortho-Clinical
Diagnostics'  professional diagnostic products. Also contributing
to   the   results  was  strong  growth  in  Biosense   Webster's
electrophysiology  business  and  in  Ethicon's  wound  care  and
women's health businesses. Growth was impacted by lower sales  of
drug-eluting stents in our Cordis franchise primarily  due  to  a
decline in the market versus the prior year.

During  the quarter, the Company received approval from the  U.S.
Food  and  Drug  Administration (FDA) for the REALIZE  Adjustable
Gastric  Band,  a  surgical implant for the treatment  of  morbid
obesity.  The FDA also approved the GENESEARCH Breast Lymph  Node
Assay, which is the first intra-operative and gene-based test  to
detect the spread of breast cancer into the lymph nodes.

Worldwide  Pharmaceutical sales of $6.1  billion  for  the  third
quarter represented an increase over the prior year of 3.7%  with
operational growth of 1.2% and a positive impact from currency of
2.5%.  Domestic  sales decreased 2.0%, while international  sales
increased 14.4% (7.2% from operations and 7.2% from currency).

Sales  growth  reflects  the strong performance  of  TOPAMAX,  an
antiepileptic  and  a  treatment for the prevention  of  migraine
headaches; our antipsychotic franchise, which includes RISPERDAL,
RISPERDAL  CONSTA  and INVEGA; and REMICADE, a biologic  approved
for  the  treatment  of a number of immune mediated  inflammatory
diseases.  Growth  was  impacted by lower  sales  of  PROCRIT,  a
product  for the treatment of anemia, primarily due to a  decline
in  the  market.  This market decline is related  to  a  labeling
change  made this past March and a decision memorandum issued  by
the  Centers for Medicare & Medicaid Services under its  national
coverage analysis process.

In  October,  the  Company received approval  from  the  FDA  for
DORIBAX  (doripenem  for  injection)  as  a  new  treatment   for
complicated   intra-abdominal  and  complicated   urinary   tract
infections,  including pyelonephritis. During  the  quarter,  the
Company filed a new drug application in both the U.S. and  Europe
for   TMC125   (etravirine),  an  investigational  non-nucleoside
reverse  transcriptase inhibitor (NNRTI), being studied  for  use
with  other  antiretroviral  agents as  a  treatment  for  people
infected with HIV-1.

Worldwide  Consumer segment sales of $3.6 billion for  the  third
quarter  represented a 47.5% increase over the  prior  year  with
operational  growth of 43.4% and a positive impact from  currency
of  4.1%.  Domestic  sales increased 39.8%,  while  international
sales  increased  54.2%  (46.5% from  operations  and  7.7%  from
currency). On a pro-forma basis, including the net impact of  the
acquisition  of  Pfizer  Consumer  Healthcare  in  both  periods,
worldwide   sales  for  the  Consumer  segment   increased   3.5%
operationally.

Sales  growth  in  the  combined  business  reflects  the  strong
performance of the LISTERINE antiseptic mouthrinse and the launch
of  whitening  products; the skin care lines of AVEENO,  CLEAN  &
CLEAR,  and  NEUTROGENA; McNeil Nutritional's SPLENDA  sweetener;
and  Baby  and  Kids  Care  products.  In  October,  the  Company
announced  it was voluntarily withdrawing certain infants'  cough
and  cold  products from the market. An assessment  of  available
data  on the use of pediatric cough and cold medicines identified
rare  instances  of misuse leading to overdose,  particularly  in
infants  under  2  years  of age. When used  as  directed,  these
medicines are generally recognized as safe and effective.

Johnson  & Johnson is the world's most comprehensive and  broadly
based manufacturer of health care products, as well as a provider
of  related  services,  for  the  consumer,  pharmaceutical,  and
medical  devices  and  diagnostics markets.  The  more  than  250
Johnson   &  Johnson  operating  companies  employ  approximately
120,000   men  and  women  in  57  countries  and  sell  products
throughout the world.

    * Net earnings and diluted earnings per share excluding after-
tax in-process research and development charges and restructuring
charges  are  non-GAAP  financial  measures  and  should  not  be
considered replacements for GAAP results. For a reconciliation of
these non-GAAP financial measures to the most directly comparable
GAAP  financial  measures, see the accompanying  tables  to  this
release.


NOTE TO INVESTORS
Johnson  & Johnson will conduct a meeting with financial analysts
to discuss this news release today at 8:30 a.m., Eastern Daylight
Time. A simultaneous webcast of the call for interested investors
and  others  may  be accessed by visiting the Johnson  &  Johnson
website  at  www.investor.jnj.com. A replay and podcast  will  be
available  approximately  two hours after  the  live  webcast  by
visiting www.investor.jnj.com.

Copies of the financial schedules accompanying this press release
are    available    at    http://www.investor.jnj.com/historical-
sales.cfm.  The  schedules include supplementary  sales  data,  a
condensed  consolidated statement of earnings, and sales  of  key
products/franchises. Additional information on Johnson &  Johnson
can be found on the Company's website at http://www.jnj.com.

(This  press  release  contains "forward-looking  statements"  as
defined in the Private Securities Litigation Reform Act of  1995.
These  statements  are  based on current expectations  of  future
events.  If  underlying assumptions prove inaccurate  or  unknown
risks  or  uncertainties materialize, actual results  could  vary
materially from Johnson & Johnson's expectations and projections.
Risks  and uncertainties include general industry conditions  and
competition;  economic  conditions, such  as  interest  rate  and
currency  exchange rate fluctuations; technological advances  and
patents  attained  by  competitors; challenges  inherent  in  new
product  development,  including obtaining regulatory  approvals;
domestic  and  foreign health care reforms and governmental  laws
and  regulations; and trends toward health care cost containment.
A  further list and description of these risks, uncertainties and
other  factors can be found in Exhibit 99 of the Company's Annual
Report on Form 10-K for the fiscal year ended December 31,  2006.
Copies  of  this  Form 10-K, as well as subsequent  filings,  are
available  online at www.sec.gov, www.jnj.com or on request  from
Johnson & Johnson. Johnson & Johnson does not undertake to update
any forward- looking statements as a result of new information or
future events or developments.)